Assessment of laboratories, records, facilities, test articles, test systems, facilities, chain of custody
for compliance with GLP regulations
Laboratory evaluation (personnel training and records, materials, experimental or analytical documentation, etc.)
Laboratory facilities (inspection of sample collection, preparation and storage procedures, analytical procedures and raw data audit, QA documentation audit, etc.)
Review SOPs for compliance with international standards
Records, reports and record/sample retention
Interested in learning whether current clinical programs, research developments, or emerging therapeutic approaches may be relevant to your situation?
Educational and research information only. Individual medical decisions should be made in consultation with qualified healthcare professionals.
